In Molecular beacon based qPCR assays, when the probe-target hybridization takes place, do quenching occur between the fluorophore of one molecular beacon molecule (in open state) and quencher of other molecular beacon molecule (in open state) since at the time of annealing, there will be multiple probe molecules bound to their complementary targets and there can be interaction between the fluorophore of probe and quencher of adjacent probe (both probes are in open state)?

If this thing happens (i.e quenching), then isn't it limiting the efficiency or advantage of Molecular Beacon probes?

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